Development of a fluorimetric method for assessing paracetamol in pharmaceuticals tablets

被引:20
作者
Perera, G. W. C. S. [1 ,2 ]
de Costa, M. D. P. [1 ]
Mahanama, K. R. R. [1 ]
机构
[1] Univ Colombo, Dept Chem, Colombo 03, Sri Lanka
[2] Inst Chem Ceylon, Rajagiriya, Sri Lanka
关键词
Paracetamol; Fluorimetric method; Oxidation; Fluorescence quenching; LIQUID-CHROMATOGRAPHIC DETERMINATION; HUMAN PLASMA; SPECTROPHOTOMETRIC DETERMINATION; DERIVATIVE SPECTROPHOTOMETRY; ACYCLOVIR; RIBAVIRIN; AMANTADINE; BLOOD; ASSAY; SERUM;
D O I
10.1016/j.jphotochem.2018.09.039
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A simple, sensitive, quick, cost effective, and reliable fluorimetric method for the determination of paracetamol has been developed. The method was based on oxidation of paracetamol by potassium chlorate in the presence of sulphuric acid followed by monitoring of the fluorescence quenching of quinine sulphate by chloride ions at the excitation wavelength of 360 nm and emission wavelength of 446 nm. The fluorescence emission was corrected with a correction factor using absorbance for every sample. All absorbances and emissions were monitored by exiting samples at lambda = 360 nm with optimized conditions. There was a linear relationship between the quantum yield ratio and the paracetamol concentration, with a correlation coefficient of 0.996. The detection limit and quantification level were 56.0 ng mL(-1) and 189.0 ng mL(-1), respectively. The precision and accuracy of the method were satisfactory and the standard deviation of recovery was not more than 2%. The amount of paracetamol estimated by the developed fluorimetric method was compared with the standard method. The percentage of weights recovery of standard paracetamol from the fluorimetric method were found to be 98 to 102% suggesting the high reliability of the developed method.
引用
收藏
页码:248 / 253
页数:6
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